Biocatalytic Feedback-Driven Temporal Programming of Self-Regulating Peptide Hydrogels

被引:211
作者
Heuser, Thomas [1 ]
Weyandt, Elisabeth [1 ]
Walther, Andreas [1 ]
机构
[1] DWI Leibniz Inst Interact Mat, D-52056 Aachen, Germany
关键词
dynamic materials; hydrogels; materials science; peptides; self-regulation; DYNAMIC INSTABILITY; ROOM-TEMPERATURE; UREA HYDROLYSIS; DESIGN; GELS; ASSEMBLIES; POLYMERS; PATHWAY; LOCKING; MOTION;
D O I
10.1002/anie.201505013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Switchable self-assemblies respond to external stimuli with a transition between near-equilibrium states. Although being a key to present-day advanced materials, these systems respond rather passively, and do not display autonomous dynamics. For autonomous behavior, approaches must be found to orchestrate the time domain of self-assemblies, which would lead to new generations of dynamic and self-regulating materials. Herein, we demonstrate catalytic control of the time domain of pH-responsive peptide hydrogelators in a closed system. We program transient acidic pH states by combining a fast acidic activator with the slow, enzymatic, feedback-driven generation of a base (dormant deactivator). This transient state can be programmed over orders of magnitude in time. It is coupled to dipeptides to create autonomously self-regulating, dynamic gels with programmed lifetimes, which are used for fluidic guidance, burst release, and self-erasing rapid prototyping.
引用
收藏
页码:13258 / 13262
页数:5
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